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Medline MDS096502P

by Medline Industries, Inc.

Medline MDS096502P is a Class I device made by Medline Industries, Inc., listed in FDA GUDID since 17 Nov 2020 (UDI-DI 10884389105641), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10884389105641 UDI-DI Date17 Nov 2020ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Medline
Generic name
Oral care swab
Model / Ref / Catalog
MDS096502P
Primary DI / UDI-DI
10884389105641
FDA product code
KXF
GMDN term
Oral care swab
Device class
Class I
Regulation number
880.6025
GUDID distribution status
In Commercial Distribution

Related devices

Category: Oral care swab

Similar devices

Also classified as Oral care swab.

Similar devices

Other devices filed under FDA product code KXF (APPLICATOR, ABSORBENT TIPPED, NON-STERILE).

Other devices from Medline Industries, Inc.

See all devices from Medline Industries, Inc. →

Properties

  • Single use
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)